Evidence map›Paper›PMID 35504881›Full record

ArticleNature communications2022

Alterations in homologous recombination repair genes in prostate cancer brain metastases.

Antonio Rodriguez-Calero, John Gallon, Dilara Akhoundova, Sina Maletti, Alison Ferguson, Joanna Cyrta, Ursula Amstutz, Andrea Garofoli, Viola Paradiso, Scott A Tomlins and 17 more

Abstract read
In one paragraph

Article in Nature communications, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

19 citing papers in PubMed.

  1. Article
  2. Article
  3. RUNX1T1 drives stem-like small-cell neuroendocrine prostate cancer identity.Frontiers in cell and developmental biology · 2026
    Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

27 authors.

Antonio Rodriguez-Calero *Department for BioMedical Research, University of Bern, Bern, Switzerland.
John Gallon *Visceral Surgery and Precision Medicine Research Laboratory, Department of Biomedicine, University of Basel, Basel, Switzerland.ORCID 0000-0002-5328-6298
Dilara AkhoundovaDepartment for BioMedical Research, University of Bern, Bern, Switzerland.
Sina MalettiDepartment for BioMedical Research, University of Bern, Bern, Switzerland.
Alison FergusonDepartment for BioMedical Research, University of Bern, Bern, Switzerland.ORCID 0000-0002-6491-996X
Joanna CyrtaDepartment of Pathology, Institut Curie, University Paris Sciences et Lettres, Paris, France.
Ursula AmstutzDepartment of Clinical Chemistry, Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland.
Andrea GarofoliInstitute of Medical Genetics and Pathology, University Hospital Basel, University of Basel, Basel, Switzerland.
Viola ParadisoInstitute of Medical Genetics and Pathology, University Hospital Basel, University of Basel, Basel, Switzerland.
Scott A TomlinsDepartments of Pathology and Urology, University of Michigan Medical School, Ann Arbor, MI, USA.
Ekkehard HewerInstitute of Pathology, University of Bern, Bern, Switzerland.ORCID 0000-0002-9128-0364
Vera GenitschInstitute of Pathology, University of Bern, Bern, Switzerland.
Achim FleischmannInstitute of Pathology, University of Bern, Bern, Switzerland.
Erik VassellaInstitute of Pathology, University of Bern, Bern, Switzerland.
Elisabeth J RushingInstitute of Neuropathology, University Hospital Zurich, Zurich, Switzerland.ORCID 0000-0001-7616-6320
Rainer GrobholzInstitute of Pathology, Cantonal Hospital Aarau, Aarau, Switzerland.ORCID 0000-0002-1901-7967
Ingeborg FischerInstitute of Pathology, Cantonal Hospital Aarau, Aarau, Switzerland.
Wolfram JochumInstitute of Pathology, Cantonal Hospital St. Gallen, St. Gallen, Switzerland.
Gieri CathomasInstitute of Pathology, Cantonal Hospital Baselland, Liestal, Switzerland.
Adeboye O OsunkoyaDepartments of Pathology and Laboratory Medicine, and Urology, Emory University School of Medicine, Atlanta, USA.ORCID 0000-0001-5712-8134
Lukas BubendorfInstitute of Medical Genetics and Pathology, University Hospital Basel, University of Basel, Basel, Switzerland.ORCID 0000-0001-5970-1803
Holger MochDepartment of Pathology and Molecular Pathology, University Hospital Zurich, Zurich, Switzerland.ORCID 0000-0002-7986-2839
George ThalmannDepartment of Urology, Inselspital, Bern University Hospital, Bern, Switzerland.
Charlotte K Y NgDepartment for BioMedical Research, University of Bern, Bern, Switzerland.ORCID 0000-0002-6100-0026
Silke GillessenFaculty of Biomedical Sciences, USI, Lugano, Switzerland.
Salvatore PiscuoglioVisceral Surgery and Precision Medicine Research Laboratory, Department of Biomedicine, University of Basel, Basel, Switzerland. s.piscuoglio@unibas.ch.ORCID 0000-0003-2686-2939
Mark A RubinDepartment for BioMedical Research, University of Bern, Bern, Switzerland. mark.rubin@dbmr.unibe.ch.ORCID 0000-0002-8321-9950

Funding

Weill Cornell Medicine (WCM) SPORE in Prostate CancerP50CA211024 · NCI · WEILL MEDICAL COLL OF CORNELL UNIV · PI LODA, MASSIMO · 2017 to 2021
$10.9M
NCI NIH HHS P50 CA211024
6 · The paper itself

Abstract

Improved survival rates for prostate cancer through more effective therapies have also led to an increase in the diagnosis of metastases to infrequent locations such as the brain. Here we investigate the repertoire of somatic genetic alterations present in brain metastases from 51 patients with prostate cancer brain metastases (PCBM). We highlight the clonal evolution occurring in PCBM and demonstrate an increased mutational burden, concomitant with an enrichment of the homologous recombination deficiency mutational signature in PCBM compared to non-brain metastases. Focusing on known pathogenic alterations within homologous recombination repair genes, we find 10 patients (19.6%) fulfilling the inclusion criteria used in the PROfound clinical trial, which assessed the efficacy of PARP inhibitors (PARPi) in homologous recombination deficient prostate cancer. Eight (15.7%) patients show biallelic loss of one of the 15 genes included in the trial, while 5 patients (9.8%) harbor pathogenic alterations in BRCA1/2 specifically. Uncovering these molecular features of PCBM may have therapeutic implications, suggesting the need of clinical trial enrollment of PCBM patients when evaluating potential benefit from PARPi.

Indexed as

Brain NeoplasmsProstatic NeoplasmsHumansMaleMutationPoly(ADP-ribose) Polymerase InhibitorsRecombinational DNA RepairPoly(ADP-ribose) Polymerase Inhibitors

Identifiers

PMID35504881
PMCPMC9065149

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.